- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03499951
Remote Wheelchair Skills Training Efficacy
July 28, 2022 updated by: Michael Boninger, University of Pittsburgh
Remote Wheelchair Skills Training Efficacy Coordinating Center
The objective of the study is to evaluate the effectiveness of remote training to teach clinicians how to train others in wheelchair skills.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
32
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Florida
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Miami, Florida, United States, 33136
- South Florida Spinal Cord Injury System
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Illinois
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Chicago, Illinois, United States, 60611
- Midwest Regional Spinal Cord Injury Care System
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New Jersey
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West Orange, New Jersey, United States, 07052
- Northern New Jersey Spinal Cord System
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Pennsylvania
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Pittsburgh, Pennsylvania, United States, 15219
- University of Pittsburgh Model Center on Spinal Cord Injury
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
• Age 18 to 75
Exclusion Criteria:
• Upper or lower extremity injury that would preclude the ability to use a wheelchair.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
OTHER: Wheelchair Skills Trainers
Individuals will receive remotely delivered wheelchair skills training, after which they will be assessed on their ability to teach the Wheelchair Skills Trainees a series of wheelchair skills in a one-on-one environment.
The intervention for this group is Wheelchair Skills Training - Remote.
|
Individuals will receive wheelchair skills training remotely.
They will be provided with the Wheelchair Skills Training Program to review (http://www.wheelchairskillsprogram.ca/eng/index.php), and then will be directed to use this information to perform the wheelchair skills.
They will video the attempts, and will receive feedback on methods to improve their techniques.
|
OTHER: Wheelchair Skills Trainees
Individuals will receive one-on-one wheelchair skills training from the Wheelchair Skills Trainers.
The intervention for this group is Wheelchair Skills Training - In Person.
|
Individuals will receive wheelchair skills training in one-on-one sessions, taught by those who received the wheelchair skills training remotely.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change from baseline in wheelchair skills capacity of trainees at study completion as measured by the Wheelchair Skills Test Questionnaire
Time Frame: Baseline, and at study completion ( an average of 3 weeks)
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Trainees will have increased capacity to perform wheelchair skills after receiving one-on-one skills training.
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Baseline, and at study completion ( an average of 3 weeks)
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Change from baseline in wheelchair skills confidence of trainees at study completion as measured by the Wheelchair Skills Test Questionnaire
Time Frame: Baseline, and at study completion ( an average of 3 weeks)
|
Trainees will have increased confidence in their ability to perform wheelchair skills after receiving one-on-one skills training.
|
Baseline, and at study completion ( an average of 3 weeks)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
May 25, 2018
Primary Completion (ACTUAL)
October 4, 2018
Study Completion (ACTUAL)
October 4, 2018
Study Registration Dates
First Submitted
March 19, 2018
First Submitted That Met QC Criteria
April 13, 2018
First Posted (ACTUAL)
April 17, 2018
Study Record Updates
Last Update Posted (ACTUAL)
July 29, 2022
Last Update Submitted That Met QC Criteria
July 28, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PRO18010289
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
There is no plan to share IPD outside of collaborators.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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